Acetaldehyde is more reactive than acetone towards addition of HCN.
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In semicarbazide, the reaction occurs via the available -NH₂ group attached to the carbonyl. Aldehydes are generally more reactive than ketones due to their less hindered electron distribution.
Acetaldehyde is more reactive than acetone towards HCN addition because acetaldehyde has a smaller electron-donating alkyl group (-CH₃) compared to acetone, making its carbonyl carbon more electrophilic and susceptible to nucleophilic attack by HCN.
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